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Bioorganic & Medicinal Chemistry Letters|April 1, 2000

Solid phase synthesis of diamides as potential bone resorption inhibitorsK M Edvinsson, M Herslöf, P Holm, et al.

Journal of Medicinal Chemistry|July 7, 1995

Reversible inhibitors of the gastric (H+/K+)-ATPase. 4. Identification of an inhibitor with an intermediate duration of actionC A Leach, T H Brown, R J Ife, et al.

European Journal of Biochemistry|June 24, 2000

Properties of three isoforms of the 116-kDa subunit of vacuolar H+-ATPase from a single vertebrate species. Cloning, gene expression and protein characterization of functionally distinct isoforms in Gallus gallusJ P Mattsson, X Li, S B Peng, et al.

Journal of Medicinal Chemistry|July 7, 1995

Reversible inhibitors of the gastric (H+/K+)-ATPase. 5. Substituted 2,4-diaminoquinazolines and thienopyrimidinesR J Ife, T H Brown, P Blurton, et al.

Journal of Medicinal Chemistry|May 15, 1992

Reversible inhibitors of the gastric (H+/K+)-ATPase. 2. 1-Arylpyrrolo[3,2-c]quinolines: effect of the 4-substituentC A Leach, T H Brown, R J Ife, et al.

Journal of Medicinal Chemistry|August 1, 1989

2-[[(4-Amino-2-pyridyl)methyl]sulfinyl]benzimidazole H+/K+-ATPase inhibitors. The relationship between pyridine basicity, stability, and activityR J Ife, C A Dyke, D J Keeling, et al.

Journal of Medicinal Chemistry|September 4, 1992

Reversible inhibitors of the gastric (H+/K+)-ATPase. 3. 3-substituted-4-(phenylamino)quinolinesR J Ife, T H Brown, D J Keeling, et al.

Journal of Medicinal Chemistry|February 1, 1990

Reversible inhibitors of the gastric (H+/K+)-ATPase. 1. 1-Aryl-4-methylpyrrolo[3,2-c]quinolines as conformationally restrained analogues of 4-(arylamino)quinolinesT H Brown, R J Ife, D J Keeling, et al.

The Journal of Biological Chemistry|April 18, 1997

Subunit G of the vacuolar proton pump. Molecular characterization and functional expressionB P Crider, P Andersen, A E White, et al.

Nature Genetics|July 11, 2000

Defects in TCIRG1 subunit of the vacuolar proton pump are responsible for a subset of human autosomal recessive osteopetrosisA Frattini, P J Orchard, C Sobacchi, et al.

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Bioorganic & Medicinal Chemistry Letters|April 1, 2000

Solid phase synthesis of diamides as potential bone resorption inhibitorsK M Edvinsson, M Herslöf, P Holm, et al.

Journal of Medicinal Chemistry|July 7, 1995

Reversible inhibitors of the gastric (H+/K+)-ATPase. 4. Identification of an inhibitor with an intermediate duration of actionC A Leach, T H Brown, R J Ife, et al.

European Journal of Biochemistry|June 24, 2000

Properties of three isoforms of the 116-kDa subunit of vacuolar H+-ATPase from a single vertebrate species. Cloning, gene expression and protein characterization of functionally distinct isoforms in Gallus gallusJ P Mattsson, X Li, S B Peng, et al.

Journal of Medicinal Chemistry|July 7, 1995

Reversible inhibitors of the gastric (H+/K+)-ATPase. 5. Substituted 2,4-diaminoquinazolines and thienopyrimidinesR J Ife, T H Brown, P Blurton, et al.

Journal of Medicinal Chemistry|May 15, 1992

Reversible inhibitors of the gastric (H+/K+)-ATPase. 2. 1-Arylpyrrolo[3,2-c]quinolines: effect of the 4-substituentC A Leach, T H Brown, R J Ife, et al.

Journal of Medicinal Chemistry|August 1, 1989

2-[[(4-Amino-2-pyridyl)methyl]sulfinyl]benzimidazole H+/K+-ATPase inhibitors. The relationship between pyridine basicity, stability, and activityR J Ife, C A Dyke, D J Keeling, et al.

Journal of Medicinal Chemistry|September 4, 1992

Reversible inhibitors of the gastric (H+/K+)-ATPase. 3. 3-substituted-4-(phenylamino)quinolinesR J Ife, T H Brown, D J Keeling, et al.

Journal of Medicinal Chemistry|February 1, 1990

Reversible inhibitors of the gastric (H+/K+)-ATPase. 1. 1-Aryl-4-methylpyrrolo[3,2-c]quinolines as conformationally restrained analogues of 4-(arylamino)quinolinesT H Brown, R J Ife, D J Keeling, et al.

The Journal of Biological Chemistry|April 18, 1997

Subunit G of the vacuolar proton pump. Molecular characterization and functional expressionB P Crider, P Andersen, A E White, et al.

Nature Genetics|July 11, 2000

Defects in TCIRG1 subunit of the vacuolar proton pump are responsible for a subset of human autosomal recessive osteopetrosisA Frattini, P J Orchard, C Sobacchi, et al.

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